NEFH and STXBP1

  • Number of citations of the paper that reports this interaction (PMID 12963086)
  • 9
  • Data Source:
  • HPRD (in vivo)

NEFH

STXBP1

Gene Name neurofilament, heavy polypeptide syntaxin binding protein 1
Image No pdb structure No pdb structure
Gene Ontology Annotations Cellular Component
Molecular Function
Biological Process
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions 5 interactors: MAPK1 NEFL NEFM PKN1 STXBP1 27 interactors: APBA1 APBA2 APP CDK5 CDK5R1 DOC2A DOC2B DYT10 HGS MAPT NEFH NEFM PLD1 PLD2 PRKCA PRKCB PRKCG SQSTM1 STX11 STX19 STX1A STX1B STX2 STX3 SYTL4 TRIM38 USO1
Entrez ID 4744 6812
HPRD ID 01204 04235
Ensembl ID ENSG00000100285 ENSG00000136854
Uniprot IDs P12036 B7Z1V5 P61764 Q68CM6
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?
carriers  certainty  cryb2  d22s268  d22s280  deafness  dominantly  gadolinium  gardner  inherited  linkage  manifestations  manifests  mri  neuro  neurofibromatosis  neurologic  nf2  ophthalmologic  otologic  pedigree  predisposes  presymptomatic  schwannomas  slowly  spine  thoroughly  typically  vestibular 
16p12  2q24  5q14  9q34  aetiology  caln1  cdkl5  cgh  cnv  cnvs  counselling  ehmt1  encephalopathies  encompassing  epileptic  etiological  grin2a  hypsarrhythmia  infantile  intronic  iss  kcnq2  magi2  mef2c  microdeletions  microduplications  scn2a  spasms  xq28 
Tagcloud (Difference) ?
carriers  certainty  cryb2  d22s268  d22s280  deafness  dominantly  gadolinium  gardner  inherited  linkage  manifestations  manifests  mri  neuro  neurofibromatosis  neurologic  nf2  ophthalmologic  otologic  pedigree  predisposes  presymptomatic  schwannomas  slowly  spine  thoroughly  typically  vestibular 
16p12  2q24  5q14  9q34  aetiology  caln1  cdkl5  cgh  cnv  cnvs  counselling  ehmt1  encephalopathies  encompassing  epileptic  etiological  grin2a  hypsarrhythmia  infantile  intronic  iss  kcnq2  magi2  mef2c  microdeletions  microduplications  scn2a  spasms  xq28 
Tagcloud (Intersection) ?